Transduction of human CD34+ cells that mediate long-term engraftment of NOD/SCID mice by HIV vectors

Science. 1999 Jan 29;283(5402):682-6. doi: 10.1126/science.283.5402.682.

Abstract

Efficient gene transfer into human hematopoietic stem cells (HSCs) is an important goal in the study of the hematopoietic system as well as for gene therapy of hematopoietic disorders. A lentiviral vector based on the human immunodeficiency virus (HIV) was able to transduce human CD34+ cells capable of stable, long-term reconstitution of nonobese diabetic/severe combined immunodeficient (NOD/SCID) mice. High-efficiency transduction occurred in the absence of cytokine stimulation and resulted in transgene expression in multiple lineages of human hematopoietic cells for up to 22 weeks after transplantation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Antigens, CD34 / analysis*
  • Bone Marrow Cells / cytology
  • Cell Division
  • Cell Survival
  • Colony-Forming Units Assay
  • Gene Expression
  • Gene Transfer Techniques*
  • Genetic Vectors*
  • Green Fluorescent Proteins
  • HIV / genetics*
  • Hematopoiesis
  • Hematopoietic Stem Cell Transplantation*
  • Hematopoietic Stem Cells* / cytology
  • Hematopoietic Stem Cells* / immunology
  • Humans
  • Leukemia Virus, Murine / genetics
  • Luminescent Proteins / genetics
  • Mice
  • Mice, Inbred NOD
  • Mice, SCID
  • Promoter Regions, Genetic
  • Transfection
  • Transgenes

Substances

  • Antigens, CD34
  • Luminescent Proteins
  • Green Fluorescent Proteins